Crustacea: Oregon cave amphipod
(Crustacea: Malacostraca: Amphipoda: Crangonyctidae)
Profile prepared by Sarah Foltz, The Xerces Society for Invertebrate Conservation
Stygobromus oregonensis is a freshwater, cavernicolous amphipod species known from a single cave near Roseburg, Oregon, where it was collected in 1967 and again in 1983. The presence of subterranean groundwater, such as in small pools at the bottom of caves and crevices, is probably the limiting factor in the distribution of this species. Little is known about its life cycle, development, ecological interactions, or population biology. Its global status is Critically Imperiled: at very high risk of extinction due to extreme rarity. The subterranean habitat of this species subjects it to a wide variety of groundwater disturbances, including pesticides applied to crops, lawns, and roadsides, and fecal waste from sewage plant effluent, septic field waste, and livestock feed-lots.
Rounded Global Status: G1 – Critically Imperiled
Nation: United States
National Status (United States): N1N2
State Status: Oregon: S1S2 (The Oregon ranking indicates that the species is imperiled to critically imperiled because of extreme rarity or some other factor(s) making it especially vulnerable to extirpation or extinction).
Amphipods are shrimp-like crustaceans with elongate, laterally compressed bodies and seven (rarely six) pairs of leg-like appendages (Triplehorn and Johnson 2005). The anterior pairs of legs are directed downward and forward, while the posterior legs are usually turned upward and backward. The abdominal segments are more or less fused with the thoracic segments, and the carapace (hard covering of the thorax common in other crustaceans) is lacking. Each of the six abdominal segments has one pair of short appendages on the underside. The cephalothorax (a fusion of the head and first thoracic segment) has two pairs of antennae. The eyes are generally well-developed but are sometimes reduced or lacking, particularly in subterranean species.
The type-series of Stygobromus oregonensis consists of two fully mature females measuring 9.5 mm (0.37 in.) and 11.0 mm (0.43 in.) in body length, excluding appendages. This relatively large species (most Stygobromus are under 10 mm (0.39 in.) in length) can be easily distinguished from other species of the hubbsi group by the following traits: numerous long, stiff setae and slender spines on peduncular segments IV and V of the second antennae; proportionately large propod of gnathopod I with very long, heavily spined palm; convex palm of gnathopodal propod II with a double row of 16 spine teeth; gnathopodal propods with doubly and triply inserted superior medial setae; posterior margins of the bases of pereopods V-VII convex; posterior marginal setae of pleonal plates II and III positioned midlaterally; pleonal plates with small, subacute posterior corners; and the comparatively large ramus of uropod III with 5 rather long spines (Holsinger 1974).
The holotype of this species is deposited in the Smithsonian’s United States National Museum of Natural History in Washington, D. C. and the paratype is in the research collection of Dr. John Holsinger at Old Dominion University, Norfolk, Virginia (Holsinger 2008, pers. comm.).
Little is known about the life cycle, development, ecological interactions, or population biology of this species. Sexually mature females have been collected in April and January, although this may be more reflective of sampling period than the phenology of the animal.
In general, amphipod eggs are deposited in a brood pouch on the underside of the adult female. The eggs hatch in one to three weeks, and the young amphipods remain in the pouch for about one to eight days. They are released the first time their mother sheds her skin after her next mating (Voshell 2002). The immature stages resemble the adults, and undergo successive molts (usually between 8 and 9) until maturity. It is unclear whether sexual maturity is reached after a fixed number of molts or the completion of gonad development, both of which have temperature dependent rates (Highsmith & Coyle 1991). Most species complete their life cycle (egg to adult) in one year or less (reviewed in Fasulo 2005). Subterranean species appear to have an exceptionally long lifespan and may live for four to six years (Voshell 2002).
Stygobromus is a relatively large genus, consisting of approximately 135 described species, most of which are from the United States (ZipcodeZoo 2008, Holsinger 1974). This species is known from a single small cave on private land near Roseburg, Douglas Co., Oregon (Holsinger 1974), where it was collected by Jim Riggs on two occasions: in April, 1967 and in January, 1983 (Holsinger 2008, pers. comm.).
Forest Service/BLM lands: There are no records of this species on federal lands.
Abundance: Two individuals of this species were collected on both sample occasions, but no abundance estimates of this species have been made.
The restricted, subterranean habitat of this species subjects it to a wide variety of freshwater disturbances. Since caves are underground drainage conduits for surface runoff, their biological communities are often subjected to significant quantities of nutrients and contaminants (Lewis 2001). Potential groundwater contaminants include:
• Herbicides and insecticides applied to crops, lawns, and roadsides
• Fertilizers applied to crops and lawns
• Human and livestock fecal waste, including sewage plant effluent, septic field waste, campground outhouses, feedlots, and grazing pastures
• Hazardous materials from accidental spills or deliberate dumping, including road salting
(Panno et al. 1998, Harvey & Skeleton 1968, Lewis 1996, reviewed in Lewis 2001).
Changes in water-table hydrology due to human development (withdrawal of excessive amounts of water from wells) and global climate change (particularly climatic variations in the amount of precipitation and rate of uptake by plants) may also impact this species.
The distribution of this species is expected to be much larger than is documented, including much of southern Oregon and possibly ranging as far south as California (Holsinger 2008, pers. comm.). Searching potential habitats (e.g. caves, seeps, wells, spring flows) is the only way to find out if this species occurs beyond its type-locality (Holsinger 2008, pers. comm.). Considering the numerous interconnecting cracks and crevices in many cave systems (particularly in karst areas with lava flow or fractured bedrock), it is very unlikely that this species is restricted to a single cave (Holsinger 2008, pers. comm.). With diligent search effort, a number of other karst species have been found well beyond their original type-localities (Holsinger 2008, pers. comm.).
Inventory: Survey subterranean groundwater habitat in southern Oregon for new population sites of this species. Address habitat in both unsurveyed and well-studied cave systems. Oregon Caves National Monument (OCNM), for example, has a record of amphipods from ~15 years ago but the specimens (probably Stygobromus) were not well preserved and are too damaged to be positively identified to species (Roth 2008, pers. comm.). Although recent (~2006 to 2007) surveys for this taxon at OCNM have been unproductive, additional survey work may be reveal this (or other) Stygobromus species (Roth 2008, pers. comm.).
Management: Protect known sites and their watersheds from activities that would damage or alter groundwater quality or hydrology.
Fasulo, T. 2005. Terrestrial amphipods or “lawn shrimp.” Publication Number: EENY-220, University of Florida. 18 Dec. 2008.
Highsmith, R.C. and K.O. Coyle. 1991. Amphipod life histories: community structure, impact of temperature on decoupled growth and maturation rates, productivity, and P:B ratios. American Zoologist 31: 861-873.
Holsinger, J.R. 1974. Systematics of the subterranean amphipod genus Stygobromus (Gammaridae), Part I: Species of the western United States. Smithsonian Contributions to Zoology, 160: 1-63.
Holsinger, John. 2008. Personal communication with Sarah Foltz.
Lewis, Julian J. 1996. The devastation and recovery of caves affected by industrialization. Proceedings of the 1995 National Cave Management Symposium, October 25-28, 1995, Spring Mill State Park, Indiana: 214-227.
Lewis, J. 2001. USDA Forest Service Conservation Assessment for Pocahontas Cave Amphipod (Stygobromus nanus). Available at:
NatureServe. 2008. “Stygobromus oregonensis.” NatureServe Explorer: An online encyclopedia of life [web application]. Feb. 2008. Version 7.0. NatureServe, Arlington, Virginia. 15 Dec. 2008
Panno., S.V., W.R. Kelly, C.P. Weibel, I.G. Krapac, and S.L. Sargent. 1998. The effects of land use on water quality and agrichemical loading in the Fogelpole Cave groundwater basin, southwestern Illinois. Proceedings of the Illinois Groundwater Consortium Eighth Annual Conference, Research on agriculture chemicals in Illinois groundwater, 215-233.
Roth, John. 2008. Personal communication with Sarah Foltz.
Triplehorn, C. and N. Johnson. 2005. Introduction to the Study of Insects. Thomson Brooks/Cole, Belmont, CA. 864pp.
Voshell J. R. 2002. A Guide to Common Freshwater Invertebrates of North America. The McDonald & Woodward Publishing Company, Blacksburg, Virginia. 442pp.
ZipcodeZoo, 2008. Stygobromus. 19 Dec. 2008.